Manager, Pharmacovigilance
Location: Karnataka, India
Industry: Life Sciences & Healthcare
Work Mode: Hybrid
Job ID: JREQ131103
Posted Date: March 4th, 2025
We are looking for a Manager, Pharmacovigilance to join our Pharmacovigilance (PV) team. This is an excellent opportunity to support the team by performing literature monitoring, assessing adverse event reports, and handling indexing and abstracting using extensive knowledge of scientific terms, medical terminology, drugs, therapeutic areas, and pharmacovigilance regulations.
Key Responsibilities:
Provide functional expertise and oversight of processes while addressing queries from the PV Operations staff
Participate in client and team meetings as required
Perform activities delegated to PV Operations staff during unplanned peaks or urgent requirements
Prepare for and respond to internal and external audits/inspections
Address client feedback and take corrective action regarding performance or process concerns
Provide project updates to Senior Management periodically
Assist the manager with operational day-to-day activities
Experience, Education, Skills, and Accomplishments:
Master’s Degree in Life Sciences, Health, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, etc.)
A degree in Dentistry/Physiotherapy/Nursing with patient exposure in a hospital-based environment is an advantage
Around 10 years of experience reviewing biomedical literature for adverse event reporting and at least 5 years of team management experience
Excellent leadership and line management skills
Strong knowledge of drug safety and the drug development process
Client-focused approach to work
Ability to manage multiple and varied tasks, prioritize workload, and ensure attention to detail
Ability to train and mentor team members
Preferred Skills:
Certification from a professional medical writer’s association
Experience with commercial and client-specific biomedical literature databases
Scientific/medical writing background
About the Team:
The PV Literature team supports multiple customers across various therapeutic areas. The team provides a supportive working environment with personalized training and opportunities to engage in different aspects of pharmacovigilance and participate in customer upgrade planning.
Hours of Work:
This is a full-time permanent position working weekdays (Monday to Friday).
Equal Opportunity:
At Clarivate, we are committed to providing equal employment opportunities for all persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations.
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